Cutting Edge: T Follicular Helper Cell Differentiation Is Defective in the Absence of Bcl6 BTB Repressor Domain Function

被引:22
|
作者
Nance, J. Philip [1 ]
Belanger, Simon [1 ]
Johnston, Robert J. [2 ]
Takemori, Toshitada [3 ]
Crotty, Shane [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, Div Vaccine Discovery, La Jolla, CA 92037 USA
[2] Genentech Inc, San Francisco, CA 94080 USA
[3] RIKEN, Res Ctr Allergy & Immunol, Yokohama, Kanagawa 2300045, Japan
来源
JOURNAL OF IMMUNOLOGY | 2015年 / 194卷 / 12期
基金
美国国家卫生研究院;
关键词
MHC CLASS-II; VIRAL-INFECTION; POZ DOMAIN; RESPONSES; MICE; SMRT; COMMITMENT; MECHANISMS; REGULATORS; COMPLEX;
D O I
10.4049/jimmunol.1500200
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T follicular helper (Tfh) cells are essential for germinal centers (GCs) and most long-term humoral immunity. Differentiation of Tfh cells depends on the transcriptional repressor B cell CLL/lymphoma 6 (Bcl6). Bcl6 mediates gene repression via the recruitment of corepressors. Currently, it is unknown how Bcl6 recruits corepressors to regulate gene expression of Tfh cells. In this article, we demonstrate, using a mutant form of Bcl6 with two BTB (bric-a-brac, tramtrack, broad-complex) mutations that abrogate corepressor binding, that the Bcl6 BTB domain is required for proper differentiation of Tfh and GC-Tfh cells in vivo. Importantly, we also observe a significant defect in GC B cell development. These results are consistent in multiple contexts, including a novel lymphocytic choriomeningitis virus nucleoprotein- specific TCR-transgenic mouse model. Taken together, these data suggest that the Bcl6 BTB domain is a key mediator of the differentiation of Tfh cells.
引用
收藏
页码:5599 / 5603
页数:5
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